chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6147109165147109166TC56GENIChomozygous115021795
6147164078147164079TG42GENIChomozygous115021803
6147164083147164084AC39GENIChomozygous115021804
6147164086147164087GT38GENIChomozygous115021805
6147164087147164088GC38GENIChomozygous115021806
6147164091147164092TC36GENIChomozygous115021807
6147164101147164102TA30GENIChomozygous115021808
6147164118147164119TC26GENIChomozygous115021809
6147164119147164120GA26GENIChomozygous115021810
6147164126147164127TC23GENIChomozygous115021811
6147164151147164152CT20GENIChomozygous115021812
6147164201147164202CT7GENIChomozygous115021814
6147126931147126932GA71GENICheterozygous128429515
6147127083147127084TC68GENICheterozygous115195905
6147127135147127136TG69GENICheterozygous115195909
6147127136147127137CT68GENICheterozygous130338623
6147127346147127347TC93GENICheterozygous115086166
6147164279147164279TA18GENIChomozygous128406644
6147164394147164395CG15GENIChomozygous115021817